I am currently working with a ncdfflowset from a large number of fcs-files (>1500).
I need to set several keywords to NA, but it seems changing keywords on this large ncdfflowset are extremely time-consuming (~30 sec. pr. sample). However, on subsets of the ncdfflowset object with 100 samples (FCS-files) the time used pr. sample is 1/10 as long.
keyword(ncfs) <- list(EXPERIMENT NAME
=NA, $SRC
=NA, $FIL
=NA,$FILNAME
=NA)
Is there any way to make this code more effective. The documentation on read.ncdfFlowSet is a bit scarce. What is the pros and cons of 'dim=3'?
Thanx in advance for any suggestions,
Anders T
Thank you so much, this is excellent! A test on our university system on a 200 frames ncdfFlowset: keyword changed instantly on the whole ncdfFlowset! I can't see why anyone would use any other flow cytometry software.
Anders T
Glad to hear! Thanks for reporting the issue.